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Clinical Trial Summary

The purpose of this study is to assess the feasibility, safety and efficacy of a combination of nebulized Formoterol and Revefenacin among patients hospitalized for AECOPD compared with standard-of-care therapy with nebulized Albuterol and Ipratropium.


Clinical Trial Description

A prospective, parallel group, randomized clinical trial in 60 patients hospitalized with the primary diagnosis of AECOPD or acute respiratory failure with a secondary diagnosis of COPD (ICD-10 codes J44.1 and J96 - J96.2 with J44.9). The plan is to: Administer standard bronchodilator protocol with nebulized Albuterol and Ipratropium every 6 hours (n=30) versus Nebulized Revefenacin 175 μg once per day and Formoterol 20 μg twice per day (n=30) for up to 7 days of treatment. Study medication will be administered by standard jet nebulizers in both groups. Investigators will: - Collect the Borg dyspnea scale twice a day during hospitalization - Record the total doses of bronchodilators per day received by each patient - Record the number of rescue doses needed per day of hospital stay - Record the lowest level of FiO2 employed on days 1, 3 and 7 of hospital stay - Record all adverse events and concurrent medications Investigators will collect: Physical Exam (Day 1, 3, 7, or ET) Serum Chemistry (Day 1, 3, 7, or ET) Hematology (Day 1, 3, 7, or ET) Chest X-Ray (Day 1). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04655170
Study type Interventional
Source University of Tennessee Graduate School of Medicine
Contact Jennifer Ferris, MSHS
Phone 865-305-7975
Email jferris@utmck.edu
Status Recruiting
Phase Phase 4
Start date December 9, 2020
Completion date March 30, 2023

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